ClinVar Miner

Submissions for variant NM_001370259.2(MEN1):c.1024del (p.Ala342fs)

dbSNP: rs1555164986
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000509058 SCV000038443 pathogenic Multiple endocrine neoplasia, type 1 1997-04-18 no assertion criteria provided literature only

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